Cytoscape Web
Click node...

Hyperinsulinism due to INSR deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
1 OMIM reference -
2 associated genes
No signs/symptoms info
Hyperinsulinism due to INSR deficiency
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation

INSR
(UniProt - OMIM)
 NPHS1
(UniProt - OMIM)
PTPRO
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
INSR
(0.68)
PTPRO


Citations in the biomedical literature:


Hyperinsulinism due to INSR deficiency
INSR
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
NPHS1 PTPRO



Hyperinsulinism due to INSR deficiency
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation

Synonym(s):
- Hyperinsulinemic hypoglycemia due to INSR deficiency
- Hyperinsulinemic hypoglycemia due to insulin receptor deficiency
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Diseases of the genitourinary system -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adolescence / young
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.